Structure of PDB 8khl Chain C Binding Site BS01
Receptor Information
>8khl Chain C (length=272) Species:
287
(Pseudomonas aeruginosa) [
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MNRQIVRSALFVPATRPERIPKALASGADRVIVDLEDAVEEGLKVEARAN
LRRFLVDTPEARVLVRINAAEHPGHADDLALCRDHAGVIGLLLPKVESAA
QVRHAAVASGKPVWPIVESARGLAALGEIAAAAGVERLSFGSLDLALDLD
LNSGSNAAEQILGHARYALLLQTRLAGLAPPLDGVYPAIQNRAGLVEAVR
FARDMGFGGLLCIHPSQVEPIHQTLMPSPAELEWARRVAEAGASGAGVFV
VDGEMVDAPVLGRARRLLERAG
Ligand information
Ligand ID
COA
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCS
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
8khl Chain C Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
8khl
Structural and functional characterization of itaconyl-CoA hydratase and citramalyl-CoA lyase involved in itaconate metabolism of Pseudomonas aeruginosa.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
F11 V12 P13 R19 K22 A23 A38 I213 H214 P215
Binding residue
(residue number reindexed from 1)
F11 V12 P13 R19 K22 A23 A38 I213 H214 P215
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0006107
oxaloacetate metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:8khl
,
PDBe:8khl
,
PDBj:8khl
PDBsum
8khl
PubMed
38677288
UniProt
Q9I562
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